Effectiveness of Four Transition Dietary Regimens in the Hospital Management of Children With Kwashiorkor.
NCT ID: NCT05015257
Last Updated: 2023-10-03
Study Results
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Basic Information
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COMPLETED
NA
32 participants
INTERVENTIONAL
2021-09-15
2023-08-31
Brief Summary
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At the Nutritional Rehabilitation and Education Center of the University Hospital of Bobo Dioulasso it was found that some SAM children whose oedema resolved under F75 in the stabilization phase, re-developed oedema as they entered the transition phase with RUTF. RUTF has the same nutritional value as F100 but contains iron unlike F100 (\<0.07 mg/100 mL). It was observed that RUTF in some cases may be associated with higher mortality, probably due to high iron content (10-14 mg/100 g), which may increase the risk of infections and the formation of free radicals, thereby increasing damage to the body's cells. Clinical trials evaluating the current guidelines for the treatment of SAM with oedema are scarce. A better understanding of the risk factors affecting the effectiveness of the nutritional therapeutic protocol for children with Kwashiorkor will be useful to improve their care.
The main objective of this study is to determine whether the use of transition phase diets (Plumpy-Nut®+F75 or F100 or alternative F75+/- CMV+ Plumpy-Nut®) affect oedema resolving in Kwashiorkor children and to investigate the underlying factors for the relapse or non-responsiveness to the therapeutic treatment.
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Detailed Description
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Severe acute malnutrition results in high mortality rates of up to half a million child deaths annually. Undernourished children are at higher risk of mortality ranging from three-times more risk among children with moderate malnutrition to 10-times in SAM children compared to well-nourished children.
The objective of this study is to determine whether the use of different transition phase diets affect oedema resolving in Kwashiorkor children and to investigate the underlying factors for the relapse or non-responsiveness to the therapeutic treatment.
Hypotheses to be tested
* The first hypothesis is that RUTF (Plumpy-Nut®) because of its content in iron may compromise the effectiveness of the transition phase in children with kwashiorkor
* The second hypothesis is that underlying factors including co-morbidities and epigenetics may explain a difference in response to therapeutic regimens
This is an open label randomized controlled trial to test the effectiveness of four used transition phase diets in Kwashiorkor children in their transition to the rehabilitation phase. The four dietary regimens that will be tested are:
1. F100;
2. RUTF+F75;
3. RUTF+alternative F75 with complex mineral-vitamin (CMV); and
4. RUTF+alternative F75 without CMV.
When it is decided to move to the transition phase, the child will be assigned to one of the treatments depending on the treatment received during the stabilization phase and the results of the appetite test. That is a child who accepts the Plumpy Nut will receive it in combination with their regimen they had during the stabilization phase. If a child does not accept Plumpy Nut, then they will received F100 regardless of their initial therapeutic food regimen.
* For those who received F75 in the stabilization phase, they will receive standard F75 + Plumpy Nut
* For those who received alternative F75 with CMV in the stabilization phase, they will receive alternative F75 with CMV + Plumpy Nut®
* For those who received alternative F75 without CMV in the stabilization phase, they will receive alternative F75 without CMV + Plumpy Nut®.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
When it is decided to move to the transition phase, the child will be assigned to one of the treatments depending on the treatment received during the stabilization phase and the results of the appetite test. That is a child who accepts the Plumpy Nut will receive it in combination with their regimen they had during the stabilization phase. If a child does not accept Plumpy Nut, then they will received F100 regardless of their initial therapeutic food regimen.
* For those who received F75 in the stabilization phase, they will receive standard F75 + Plumpy Nut
* For those who received alternative F75 with CMV in the stabilization phase, they will receive alternative F75 with CMV + Plumpy Nut®
* For those who received alternative F75 without CMV in the stabilization phase, they will receive alternative F75 without CMV + Plumpy Nut®.
TREATMENT
NONE
Study Groups
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Standard F100
If the test of appetite at the end of the stabilization phase is negative (the child does not accept the Plumpynut)
Standard F100
100 kcal and 3 g protein per 100 ml
Standard F75+Plumpynut
If the test of appetite at the end of the stabilization phase is positive (the child accepts the Plumpynut) and the child received Standard F75 during the stabilization phase
Standard F75 + Plumpynut
Standard F75 with ready to-use therapeutic food (Plumpynut)
Alternative F75 with CMV +Plumpynut
If the test of appetite at the end of the stabilization phase is positive (the child accepts the Plumpynut) and the child received Alternative F75 with CMV during the stabilization phase
Alternative F75 with CMV + Plumpynut
Alternative F75 containing CMV with ready to-use therapeutic food (Plumpynut)
Alternative F75 without CMV +Plumpynut
If the test of appetite at the end of the stabilization phase is positive (the child accepts the Plumpynut) and the child received Alternative F75 without CMV during the stabilization phase
Alternative F75 without CMV + Plumpynut
Alternative F75 with no CMV with ready to-use therapeutic food (Plumpynut)
Interventions
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Standard F100
100 kcal and 3 g protein per 100 ml
Standard F75 + Plumpynut
Standard F75 with ready to-use therapeutic food (Plumpynut)
Alternative F75 with CMV + Plumpynut
Alternative F75 containing CMV with ready to-use therapeutic food (Plumpynut)
Alternative F75 without CMV + Plumpynut
Alternative F75 with no CMV with ready to-use therapeutic food (Plumpynut)
Eligibility Criteria
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Inclusion Criteria
* Who are admitted and treated in the refeeding center (CREN) of the CHUSS
* Aged between 6 and 59 Months
* Parental Signed informed consent form
* Recruited in the first phase of the treatment and successfully admitted to the transition phase
Exclusion Criteria
* Moderate acute malnutrition (MAM)
* Did not improve during the stabilization phase
6 Months
59 Months
ALL
No
Sponsors
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Institut de Recherche en Sciences de la Sante, Burkina Faso
OTHER_GOV
University Hospital Sourô Sanou of Bobo Dioulasso (Burkina Faso)
UNKNOWN
Centre Muraz
OTHER
University Ghent
OTHER
Responsible Party
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Principal Investigators
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Stefaan De Henauw, Md. PhD
Role: PRINCIPAL_INVESTIGATOR
University Ghent
Souheila Abbeddou, MSc. PhD
Role: PRINCIPAL_INVESTIGATOR
University Ghent
Jerome Some, Md. PhD
Role: PRINCIPAL_INVESTIGATOR
Institut de Recherche en Sciences de la Sante, Burkina Faso
Bintou Sanogo, MSc. Md.
Role: PRINCIPAL_INVESTIGATOR
Centre Hospitalier Universitaire Souro, Bobo Dioulasso, Burkina Faso.
Locations
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Centre Hospitalier Universitaire Souro
Bobo-Dioulasso, Bobo Dioulasso, Burkina Faso
Countries
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References
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Gopalan C. Kwashiorkor and marasmus: evolution and distinguishing features. 1968. Natl Med J India. 1992 May-Jun;5(3):145-51. No abstract available.
Nguefack F, Adjahoung CA, Keugoung B, Kamgaing N, Dongmo R. [Hospital management of severe acute malnutrition in children with F-75 and F-100 alternative local preparations: results and challenges]. Pan Afr Med J. 2015 Aug 31;21:329. doi: 10.11604/pamj.2015.21.329.6632. eCollection 2015. French.
Singh K, Badgaiyan N, Ranjan A, Dixit HO, Kaushik A, Kushwaha KP, Aguayo VM. Management of children with severe acute malnutrition: experience of Nutrition Rehabilitation Centers in Uttar Pradesh, India. Indian Pediatr. 2014 Jan;51(1):21-5. doi: 10.1007/s13312-014-0328-9. Epub 2013 Jul 5.
Smith MI, Yatsunenko T, Manary MJ, Trehan I, Mkakosya R, Cheng J, Kau AL, Rich SS, Concannon P, Mychaleckyj JC, Liu J, Houpt E, Li JV, Holmes E, Nicholson J, Knights D, Ursell LK, Knight R, Gordon JI. Gut microbiomes of Malawian twin pairs discordant for kwashiorkor. Science. 2013 Feb 1;339(6119):548-54. doi: 10.1126/science.1229000. Epub 2013 Jan 30.
Related Links
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World Health Organization (2013) WHO guideline: updates on the management of severe acute malnutrition in infants and children
Enquête Nutritionnelle Nationale SMART 2016 au Burkina Faso. 2016 ; 47p
Ministère de la Sante au Burkina Faso. Protocol National : Prise en charge intégrée de la malnutrition aigüe (PCIMA). 2014
Other Identifiers
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BC-09443-B
Identifier Type: -
Identifier Source: org_study_id
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